The Safety Rates Drug Report

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Drug     Injury     Quarter    

Person who experienced the adverse event (patient)

Event ID CASEID CASEVERSION I F COD EVENT DT MFR DT INIT FDA DT FDA DT REPT COD AUTH NUM MFR NUM MFR SNDR LIT REF AGE AGE COD AGE GRP GNDR COD E SUB WT WT COD REPT DT TO MFR OCCP COD REPORTER COUNTRY OCCR COUNTRY
126671931 12667193 1 I 20150921 20160722 20160819 20160819 PER US-AJANTA PHARMA USA INC.-1056501 AJANTA PHARMA 47.00 YR F Y 0.00000 20160819 CN US US

Drug(s) used by person

Event ID CASEID DRUG SEQ ROLE COD DRUGNAME PROD AI VAL VBM ROUTE DOSE VBM CUM DOSE CHR CUM DOSE UNIT DECHAL RECHAL LOT NUM EXP DT NDA NUM DOSE AMT DOSE UNIT DOSE FORM DOSE FREQ
126671931 12667193 1 PS MONTELUKAST SODIUM. MONTELUKAST SODIUM 1 203432
126671931 12667193 2 SS VENLAFAXINE VENLAFAXINE HYDROCHLORIDE 1 Oral 0 75 MG TABLET BID
126671931 12667193 3 C LAMOTRIGINE. LAMOTRIGINE 1 0 200 MG
126671931 12667193 4 C LEVOTHYROXINE. LEVOTHYROXINE 1 0 125 UG
126671931 12667193 5 C LEVOCETIRIZINE HYDROCHLORIDE LEVOCETIRIZINE HYDROCHLORIDE 1 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
126671931 12667193 1 Seasonal allergy

Outcome of event

no results found

Reactions reported

Event ID CASEID DRUG REC ACT PT
126671931 12667193 Diarrhoea
126671931 12667193 Feeling abnormal
126671931 12667193 Headache
126671931 12667193 Hypersensitivity
126671931 12667193 Muscle spasms
126671931 12667193 Nausea
126671931 12667193 Tremor

Reporting Sources (this data is often not reported and may therefore be missing here)

no results found

Therapies reported

Event ID CASEID DSG DRUG SEQ START DT END DT DUR DUR COD
126671931 12667193 2 20150921 0